Article

In silico identification of the rare-coding pathogenic mutations and structural modeling of human NNAT gene associated with Anorexia Nervosa

2022-04-11

Abstract excerpt

<title>Abstract</title> <p><bold>Purpose</bold> Increase susceptibility towards <italic>Anorexia nervosa</italic> (AN) was reported with reduced levels of NNAT gene. We sought to investigate the most pathogenic rare-coding missense mutations (nsSNPs) of NNAT and their potential damaging impact on protein function through transcript level sequence and structure based <italic>in silico</italic> approaches. Methods...

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Literature Corpus work: 3d7809b4-c9e6-5511-b78e-6ca0f1af5f2e
DOI: 10.21203/rs.3.rs-1521353/v1

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